Quantitative determination method for chloride ions

• US 5,962,248 A
• Filed: 01/23/1996
• Issued: 10/05/1999
• Est. Priority Date: 08/04/1993
• Status: Expired due to Fees

• Current Assignee: Kyowa Medex Co., Ltd. (Resonac Holdings Corp.)
• Original Assignee: Kyowa Medex Co., Ltd. (Resonac Holdings Corp.)
• Inventors: Kayahara, Norihiko, Umemoto, Jun, Tadano, Toshio
• Primary Examiner(s): GITOMER, RALPH J
• Application Number:
  US08/586,785
• Time in Patent Office: 1,351 Days
• Field of Search: 435/14, 435/15, 435/7.22, 435/22, 435/962
• US Class Current: 435/22
• CPC Class Codes: C12Q 1/40 involving amylase

Abstract

Chloride ion is quantitatively determined in a sample by adding to the sample an enzyme having glucokinase activity to thereby eliminate glucose, admixing an α-amylase which has been deactivated by a chelating agent, and reacting the α-amylase with maltotetraose, maltohexaose or maltoheptaose.

Claims

1. A method for quantitatively determining chloride ion in a sample, comprising the steps of:

(1) admixing (i) an enzyme having a glucokinase activity, (ii) adenosine triphosphate and (iii) an aqueous medium comprising said sample;

(2) reacting said sample with said enzyme to eliminate any glucose coexisting in said sample, to obtain mixture (A);

(3) admixing mixture (A) with (i) an α

-amylase which has been deactivated by a chelating agent and (ii) a chelating agent to deactivate the enzyme having a glucokinase activity, to obtain mixture (B);

(4) reacting said α

-amylase of mixture (B) with a naturally occurring oligosaccharide selected from the group consisting of maltotetraose, maltohexaose and maltoheptaose;

(5) determining an amount of glucose produced in the reaction of step (4); and

(6) correlating said amount of glucose with a quantity of chloride ion in said sample.

2. The method of claim 1, wherein said α

-amylase is derived from porcine pancreas.

3. The method of claim 1, wherein said enzyme having a glucokinase activity is hexokinase.

5. The method of claim 1, wherein chloride ion is determined without using two-point calibration.

6. The method of claim 1, wherein a concentration of said chelating agent in step (3) is 10-50 mM.

7. The method of claim 1, wherein said chelating agent is selected from the group consisting of ethylenediaminetetraacetic acid (EDTA), 2-hydroxyethylethylenediaminetriacetic acid (HEDTA), ethylene glycol-bis(2-aminoethyl ether)tetraacetic acid (EGTA), diethylenetriaminepentaacetic acid (DTPA) and 1,2-diaminocyclohexanetetraacetic acid (DCTA).

8. The method of claim 1, wherein said oligosaccharide is added to mixture (B) in a concentration of 2-10 mM.

9. The method of any one of claims 1-8, wherein glucose is correlated with chloride ion using a calibration curve that substantially passes through its origin.

4. The method of claim 4, wherein said enzyme having a glucokinase activity is hexokinase type IV.